Search Results - Dagnino, Raymond

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  1. 1
    Design and Synthesis of a Series of Non-Peptide High-Affinity Human Corticotropin-Releasing Factor1 Receptor Antagonists

    Design and Synthesis of a Series of Non-Peptide High-Affinity Human Corticotropin-Releasing Factor1 Receptor Antagonists by Chen, Dagnino, Raymond, De Souza, Errol B, Grigoriadis, Dimitri E, Huang, Charles Q, Kim, Kyung-Il, Liu, Zhengyu, Moran, Terry, Webb, Thomas R, Whitten, Jeffrey P, Xie, Yun Feng, McCarthy, James R

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  2. 2
    1-Alkyl-3-amino-5-aryl-1H-[1,2,4]triazoles: Novel synthesis via cyclization of N-acyl-S-methylisothioureas with alkylhydrazines and their potent corticotropin-releasing factor-1 (CRF1) receptor antagonist activities

    1-Alkyl-3-amino-5-aryl-1H-[1,2,4]triazoles: Novel synthesis via cyclization of N-acyl-S-methylisothioureas with alkylhydrazines and their potent corticotropin-releasing factor-1 (C... by CHEN CHEN, DAGNINO, Raymond JR, HUANG, Charles Q, MCCARTHY, James R, GRIGORIADIS, Dimitri E

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  3. 3
    Automated synthesis of peptide C-terminal aldehydes

    Automated synthesis of peptide C-terminal aldehydes by Murphy, Aileen M, Dagnino, Raymond, Vallar, Pureza L, Trippe, Anthony J, Sherman, Shannon L, Lumpkin, Richard H, Tamura, Susan Y, Webb, Thomas R

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  4. 4
    Corrigendum to “1-Alkyl-3-amino-5-aryl-1H-[1,2,4]triazoles: Novel synthesis via cyclization of N-acyl-S-methylisothioureas with alkylhydrazines and their potent corticotropin-releasing factor-1 (CRF1) receptor antagonist activities” [Bioorg. Med. Chem. Lett. 11 (2001) 3165–3168]

    Corrigendum to “1-Alkyl-3-amino-5-aryl-1H-[1,2,4]triazoles: Novel synthesis via cyclization of N-acyl-S-methylisothioureas with alkylhydrazines and their potent corticotropin-relea... by Chen, Chen, Dagnino, Raymond, Huang, Charles Q., McCarthy, James R., Grigoriadis, Dimitri E.

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  5. 5
    Corrigendum to “1-Alkyl-3-amino-5-aryl-1 H-[1,2,4]triazoles: Novel synthesis via cyclization of N-acyl- S-methylisothioureas with alkylhydrazines and their potent corticotropin-releasing factor-1 (CRF1) receptor antagonist activities” [Bioorg. Med. Chem. Lett. 11 (2001) 3165–3168]

    Corrigendum to “1-Alkyl-3-amino-5-aryl-1 H-[1,2,4]triazoles: Novel synthesis via cyclization of N-acyl- S-methylisothioureas with alkylhydrazines and their potent corticotropin-rel... by Chen, Chen, Dagnino, Raymond, Huang, Charles Q., McCarthy, James R., Grigoriadis, Dimitri E.

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  6. 6
    A Convenient Synthetic Method for Trisubstituted s-Triazines

    A Convenient Synthetic Method for Trisubstituted s-Triazines by Chen, Chen, Dagnino, Raymond, McCarthy, James R

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  7. 7
    1-Alkyl-3-amino-5-aryl-1 H-[1,2,4]triazoles: novel synthesis via cyclization of N-Acyl- S-methylisothioureas with alkylhydrazines and their potent corticotropin-Releasing factor-1 (CRF 1) receptor antagonist activities

    1-Alkyl-3-amino-5-aryl-1 H-[1,2,4]triazoles: novel synthesis via cyclization of N-Acyl- S-methylisothioureas with alkylhydrazines and their potent corticotropin-Releasing factor-1... by Chen, Chen, Dagnino, Raymond, Huang, Charles Q., McCarthy, James R., Grigoriadis, Dimitri E.

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  8. 8
    Market watch

    Market watch by Dagnino, George, DeVoe, Raymond F, Berger, Michael, Rabbitt, Paul

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